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Biophysics and Soft Matter Seminar
Mitochondrial dynamics in neurodegenerative disorders
Gordon Rintoul
Department of Biological Sciences, ¶¡ÏãÔ°AV
Mitochondrial dynamics in neurodegenerative disorders
Feb 04, 2019 at 1:30PM
Synopsis
Mitochondria are polymorphic, dynamic organelles that play pivotal roles
in the life and death processes of eukaryotic cells. They display great
heterogeneity in number, shape and location in the cellular milieu for
different cell types, appearing as large reticular networks in some
cells and as small, punctate, autonomous organelles in others.
Non-dividing cells have mitochondria that fuse and divide and, in
neurons, they are transported along axons and dendrites. The state of
these organelles is determined by an amalgam of processes; mitochondrial
biogenesis, fission, fusion, transport and degradation. The mechanisms
by which these processes are regulated, and the mechanics of the
processes themselves, are poorly understood. However many recent studies
have implicated dysregulation of mitochondrial dynamics in neuronal
injury.
Leber hereditary optic neuropathy (LHON) is an inherited form of
blindness that is the result of degeneration of the optic nerve. The
disease has been linked to specific mutations in mitochondrial DNA. LHON
is the most common form of mitochondrial DNA disorder and there is
currently no treatment which halts the disease. Interestingly, in LHON,
a mother will pass the mutation to all of her children, but only 50% of
male and 10% of female children will suffer vision loss. It is unknown
how these mutations cause the nerve death involved in vision loss, and
why individuals who possess the mutation do not always develop vision
loss. We are exploring the cell biology of LHON through examination of
cells from LHON patient tissue biopsies. We hypothesize that cultured
human fibroblasts expressing mitochondrial mutations responsible for
LHON will demonstrate impaired cellular homeostatic mechanisms and
altered mitochondrial dynamics. I will be presenting our latest results
examining the role of mitochondria in LHON and the mechanics of changes
in mitochondrial dynamics. Findings from these studies may provide
insights into the role of mitochondria in other neurodegenerative
disorders.